[冠心病患者外周血单核细胞的促炎细胞因子和信号通路]。

Klinicheskaia meditsina Pub Date : 2017-01-01
A V Logatkina, V S Nikiforov, S S Bondar, I V Terekhov
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引用次数: 0

摘要

目的:探讨冠心病(CHD)患者外周血单核细胞(MNC)含量及其功能状态和细胞因子产生的相关因素。材料与方法:采用免疫酶法测定MNC裂解液中蛋白激酶JNK1/2、ERK1/2、MAPK38、AKT1、JAK2、FAK、AMPK、p70S6K、STAT3、STAT5B、STAT6的浓度。测定血清白细胞介素1β、2、4和y-干扰素水平。结果:用力型心绞痛和不稳定型心绞痛患者JNK水平分别比正常人高59.8%和53.1% (p < 0.05) (p < 0.05)。核转录因子水平分别为26.9%(0.015)和27.9% (0.017),JAK2 31.5%(0.022)和48.6% (0.018),STAT3 49.6%(0.025)和55.3% (0.02),STAT5B 21.5%(0.018)和30.2%(0.011)。这些变化与STAT6水平上升13.1%(0.047)和51.4%(0.019)、FAK水平上升30.1%(0.025)和79.4%(0.03)、7.6%(0.09)和15.2% (0.039)АКТ1水平、65.3(0.02)和76.2% (0.017)p70S6K水平升高相关。结论:研究结果表明,冠心病患者全血细胞持续的促炎激活是由于MNC中MAPK/SAPK信号通路成分IL-1和IL-2水平的升高以及决定细胞对IL-10敏感性的STAT3水平的降低。细胞内ERK和JNK水平的升高是MNC对促炎细胞因子的高反应性的原因。
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[PROINFLAMMATORY CYTOKINES AND SIGNALING PATHWAYS IN PERIPHERAL BLOOD MONONUCLEAR CELLS IN PATIENTS WITH CORONARY ARTERY DISEASE].

Aim: To determine content of mononuclear ells (MNC) in peripheral blood of patients with coronary heart disease (CHD) and factors responsible for their functional state and cytokine production.

Materials and methods: Concentration of proteinkinases JNK1/2, ERK1/2, MAPK38, AKT1, JAK2, FAK, AMPK, p70S6K, STAT3, STAT5B and STAT6 was determined in MNC lysate by immune-enzyme assay. Interleukin 1β, 2, 4 and y-interferon levels were measured in blood sera.

Results: In patients with angina of effort and unstable angina, the JNK level was 59,8% and 53,1% higher than the normal one respectively (р=0,013) and (р=0,012). The level of the nuclear transcription factor was 26,9% (р=0,015) and 27,9% (р=0,017), JAK2 31,5% (р=0,022) and 48,6% (р=0,018), STAT3 49,6% (р=0,025) and 55,3% (р=0,02), STAT5B 21,5% (р=0,018) and 30,2% (р=0,011) lower. These changes were associated with a 13,1% (р=0,047) and 51,4% (р=0,019) rise in the STAT6 level, 30,1% (р=0,025) and 79,4% (р=0,003) FAK level, 7,6% (р=0,09) and 15,2% (р=0,039) АКТ1 level, 65,3 (р=0,02) and 76,2% (р=0,017) p70S6K level.

Conclusion: Results of the study suggest persistent pro-inflammatory activation of whole blood cells in CHD patients due to enhanced levels of IL-1 and IL-2, components of the MAPK/SAPK signal pathway in MNC and decreased STAT3 level determining cell sensitivity to IL-10. The elevated intracellular level of ERK and JNK us responsible for high responsiveness of MNC to pro-inflammatory cytokines.

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